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G.P.1.14 A novel form of severe childhood autosomal recessive sensory neuropathy associated with optic atrophy and deafness maps to chromosome 8 q24.22-term

✍ Scribed by M. Srour; M.I. Shevell; B. Brais


Book ID
116793458
Publisher
Elsevier Science
Year
2008
Tongue
English
Weight
60 KB
Volume
18
Category
Article
ISSN
0960-8966

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